BRPI0618779B1 - absorbent articles comprising an acid superabsorbent and an organic zinc salt - Google Patents

Abstract

absorbent articles comprising an acid superabsorbent and an organic zinc salt. The present invention relates to an absorbent article, such as a diaper, a daily sanitary napkin, a female absorbent or a urinary incontinence diaper, comprising a liquid-permeable topsheet, a liquid-impermeable backsheet and an absorbent core situated between the two. above-mentioned layers, wherein it comprises a superabsorbent material, characterized in that said superabsorbent material is an acid superabsorbent material having a pH of 5.5 or less, and that the absorbent core additionally comprises an organic zinc salt. , in particular zinc ricinoleate. The combination of organic zinc salt and acid superabsorbent exerts a synergistic effect on the elimination of unpleasant basic odors such as ammonia.

Description

FIELD OF THE INVENTION The present invention relates to an absorbent article, such as a diaper, a daily sanitary napkin, a female tampon, or a urinary incontinence diaper, comprising an absorbent diaper system. Effective odor control. In particular, the present invention relates to absorbent articles wherein an acid superabsorbent material and an organic zinc salt such as zinc ricinoleate interact synergistically to reduce unpleasant odors such as ammonia.

TECHNICAL BACKGROUND

An important area of development in the area of absorbent articles of the aforementioned type is the control of unpleasant odor compounds that typically form upon release of body fluids, especially over a longer period of time. These compounds include fatty acids, ammonia, amine, sulfur containing compounds and ketones and aldehydes. They are present as natural components of body fluids, or result from the degradation processes of natural ingredients such as urea, in which microorganisms that occur in the urogenital flora often participate.

There are several approaches to suppressing unpleasant odor formation in absorbent articles. WO97 / 46188, WO97 / 46190, WO97 / 46192, WO97 / 46193, WO97 / 46195 and WO97 / 46196 disclose, for example, the incorporation of odor inhibiting or deodorant additives such as zeolites and silica. Absorption of body fluids, however, reduces the odor-inhibiting ability of zeolites as soon as they become saturated with water, as mentioned, for example, in WO98 / 17239.

A second approach involves the addition of lactobacillus with the intention of inhibiting the bacteria responsible for the unpleasant odor formation in the product. The incorporation of lactobacil and its favorable effect are disclosed, for example, in SE 9703669-3, SE 9502588-8, WO92 / 13577, SE 9801951-6 and SE 9804390-4.

Furthermore, WO98 / 57677, WO00 / 35503 and WO00 / 35505 disclose that partially neutralized superabsorbent materials (acid superabsorbent materials) counteract the formation of unpleasant odors in absorbent articles. However, acid superabsorbent materials absorb smaller amounts of body fluid as compared to common superabsorbent materials (also referred to as superabsorbent polymer, SAP).

Therefore, there is a permanent demand in the art for effective odor control systems in absorbent articles. Specifically, it would be desirable to provide an odor control system that would reduce the amount of acid SAP used. DE 10256569 A1 relates to cross-linking water-absorbing polymers containing acidic groups mainly in the form of open cell foam comprising at least one odor control agent selected from compounds with an anhydride group, compounds with an acidic group, cyclodextrans, bactericides and surfactants with an HLB value of less than 12. An example of a bactericidal compound is zinc compounds such as zinc chloride. Open cell foams according to DE 10256569 A1 to which the odor control agent may be added do not represent acid superabsorbents. In addition, no organic zinc salt is mentioned in this reference. US 2004/0180093 A1 relates to a polymer composition including an amine-containing hydrophilic polymer and a bioactive agent selected from silver, copper and zinc compounds. Known examples for zinc compounds include various inorganic salts such as zinc acetate and zinc lactate. This polymer composition is used in medical articles as dressings.

Acid superabsorbents are not mentioned. US 2004/0024374 A1 is in the name of the present applicant and relates to an absorbent article having a skin care composition applied to at least a portion thereof. One of many examples of skin care substances is zinc ricinoleate.

The highly absorbent polymers (SAPs) mentioned in this document are not specified throughout. DE 20 2004 015 738 IU describes an absorbent agent for the absorption of moisture and / or odor, characterized in that the absorbent agent consists of a mixture of active carbon and a superabsorbent. Active charcoal can be treated with zinc ricinoleate.

Acid superabsorbents are not mentioned in this document. DE 199 29 106 A1 relates to a diaper comprising an absorbent body and an associated absorbing agent, characterized in that this adsorbent is capable of adsorbing ammonia. According to the teachings of this document, this can be accomplished using partially neutralized SAPs (acids) from polyacrylic acids. According to one embodiment, zinc salt impregnated active carbon may also be present. Organic zinc salts are not mentioned in this document.

US 2002/0128621 A1, US 6,503,526 B1 and WO00 / 10500 also mention zinc salts with respect to absorbent articles, however, as a skin care agent in lotions applied on the liquid permeable cover of such absorbent articles. . From the teachings of other technical areas, it is well known that organic zinc salts of hydroxylated unsaturated fatty acids, such as zinc ricinoleate, are active deodorizing ingredients (see, for example, DE 1792074 Al, DE 2548344 Al and DE 3808114 Al ). It is a technical object of the present invention to remedy the shortcomings discussed above with respect to the state of the art.

Another technical objective is to provide an absorbent article that has an efficient odor control system. It is a further technical object of the present invention to considerably reduce or eliminate ammonia formation in absorbent articles.

BRIEF DESCRIPTION OF THE INVENTION The present invention relates to an absorbent article such as a diaper, a daily sanitary napkin, an internal absorbent, a female absorbent or a urinary incontinence diaper, comprising a liquid permeable topsheet, a liquid impervious backsheet and an absorbent core situated between the two aforementioned layers, wherein it comprises a superabsorbent material, characterized in that said superabsorbent material is an acid superabsorbent material having a pH of 5.5 or less, and that the absorbent core comprises additionally an organic zinc salt.

In the present application, acid superabsorbent material (SAP) having a pH value of 5.5 or less is often referred to simply as an acid superabsorbent material (SAP).

The present inventors have observed that an acid superabsorbent material and an organic zinc salt such as zinc ricinoleate interact synergistically in suppressing unpleasant odors and, based on this observation, have completed the present invention.

DETAILED DESCRIPTION OF THE INVENTION

Throughout the present application and claims, the use of the term "comprising" is intended to cover the more restrictive meanings as well, such as "consisting essentially of" and "consisting".

By "absorbent article" is meant articles capable of absorbing body fluids such as urine, pasty feces, female discharge or menstrual fluids. These absorbent articles include, but are not limited to, diapers, daily sanitary pads, tampons, women's pads, or diapers for urinary incontinence (as used, for example, for adults).

Such absorbent articles have a liquid permeable top layer which during use is in contact with the wearer's body. They further comprise a liquid impermeable bottom layer, for example a plastic film, a plasticized nonwoven or a hydrophobic nonwoven and an absorbent core situated between the two aforementioned layers.

A suitable topsheet may be made from a wide variety of materials, such as woven or nonwoven (e.g., a nonwoven fiber web), polymeric materials such as open plastic films, e.g. open formed thermoplastic films and films. hydroformed thermoplastics; porous foams; reticulated foams; cross-linked thermoplastic films; and thermoplastic scrims. Suitable woven and nonwoven materials may be comprised of natural fibers (e.g. wood or cotton fibers), synthetic fibers (e.g. polymeric fibers such as polyester, polypropylene or polyethylene fibers) or a combination of natural and synthetic fibers . Where the topsheet comprises a nonwoven web, it may be produced by a wide variety of known techniques (eg continuous spinning, carded spinning, wet spinning, blowing spinning, hydroentangling, combinations of the foregoing or the like). ). According to the invention, it is preferred to use open plastic films (e.g. thermoplastic films) or non-woven materials based on synthetic fibers, for example those made of polyethylene or polypropylene homo or copolymers and polymer compositions based on same.

Optionally there is at least one additional layer between the absorbent core and the top layer which may be made from a hydrophobic or hydrophilic mat or from foam materials. By "foam material" is meant cohesive flat fiber base structures of the tissue, woven or nonwoven type. The nonwoven material may have the same characteristics as described above for the upper layers.

Specifically, the at least one additional layer may contribute to directing the fluid, for example in the form of at least one absorption / distribution layer.

Such structures are taught, for example, in US 5,558,655, EP 0 640 330 Al, EP 0 631 768 Al or WO 95/01147. "Foam materials" are also well known in the art and are described, for example, in EP 0 878 481 A1 or EP 1 217 978 A1, also in the name of the present applicant. The absorbent core, which may be partially or fully coated by a core shell, comprises an acid superabsorbent material, optionally mixed with any other absorbent material that is normally compressible, adaptable, non-irritating to the wearer's skin, and capable of absorbing. and retain fluid such as urine and other body exudates.

Examples of other absorbent materials include a wide variety of liquid absorbent materials commonly used in disposable diapers and other absorbent articles, such as finely divided wood pulp, which is commonly referred to as air felt or fluff, as well as crepe liner. of cellulose; melt blown polymers, including co-form; chemically hardened, modified or cross-linked cellulosic fibers; tissue, including paper towels and laminate fabrics, absorbent foams, absorbent sponges, non-acidic superabsorbent polymers (such as superabsorbent fibers), absorbent gelling materials, or any other known absorbent materials, or combinations of materials. The term "superabsorbent material" is well known in the art and is meant water-insoluble, water-insoluble materials, capable of absorbing multiple of their own weight in body fluids. Preferably, the superabsorbent material is capable of absorbing at least 10 times its weight, preferably at least about 15 times its weight, in particular at least about 20 times its weight in an aqueous solution containing 0.9% w / w chloride sodium (measurement under normal conditions where the superabsorbent surface is freely accessible to the liquid to be absorbed). To determine the absorption capacity of superabsorbent material, the EDANA WSP 241.2 standard test may be used. The superabsorbent material may be in any form suitable for use in absorbent articles, including particles, fibers, flakes, spheres and the like, with particulate form being preferred. Acid SAPs are based on homo- or copolymers comprising at least one polymerizable unit having an acid group (e.g., a carboxylic acid group or a sulfonic acid group) such as methacrylic acid, acrylic acid, maleic acid, vinyl sulfonic acid. Corresponding polymers include, but are not limited to poly (meth) acrylic acids, ethylene maleic anhydride copolymers, vinyl sulfonic acid polymers and copolymers, polyacrylates, acrylic acid modified starch and isobutylene maleic anhydride copolymers. These polymers are preferably crosslinked so that the materials produced are substantially water insoluble. According to a preferred embodiment of the present invention, the superabsorbent material is a crosslinked homo- or copolymer comprising (meth) acrylic acid units, for example of the type disclosed in EP 0 391 108 A2. The acid superabsorbent preferably has a pH value of 3.0 to 5.5, more preferably 3.5 to 5.3, and most preferably 4.1 to 5.2. The pH is measured using the EDANA WSP 200.2 standard test.

Unlike standard SAPs, which have a pH of, for example, in the range of 5.8 or higher, the acidic SAPs used in the present invention have a pH of 5.5 or lower, with preferred ranges as defined in the previous paragraph. .

There are two ways to produce acid SAP. One is to add an acid, eg citric acid, to a standard SAP, thereby reducing the pH. The other method is to maintain a low degree of neutralization. A standard SAP has a high percentage (usually at least 70%) of the neutralized acid groups upon formation of alkali metal salts. In contrast, acidic SAPs manufactured by this method have a lower degree of neutralization, typically 15 to 60%. The degree of neutralization and pH are strongly interrelated and, as a consequence, the acidity of SAP can be controlled by the degree of neutralization.

In view of the foregoing, it is also preferred that the absorbent core comprising the acid superabsorbent has a pH value of 3.0 to 5.7, more preferably 3.5 to 5.5, in particular 4.1 to 5.4, after humidification with synthetic urine. The pH of the absorbent core can be measured very precisely with the following method, involving the preparation of an absorbent core for testing and pH measurement using it. Method 1: Preparation of absorbent cores for testing Absorbent cores were obtained from an absorbent core produced in a pilot plant. A standard method of forming a small core mat was used in core production in the pilot plant. The absorbent core consisted of a homogeneous mixture of fluffed pulp and superabsorbent material. The absorbent core was compressed to a volume of about 8-10 cm 3 / g. The sample size of the cores was 5 cm in diameter and the weight of the cores about 1.2 g. Method 2: Measurement of pH in an absorbent core An absorbent core having a diameter of approximately 50 mm was prepared according to Method 1. A predetermined amount of test liquid 1 was added, 16 ml for all samples, in Then the absorbent core was left to swell for 30 minutes.

Immediately afterwards, the pH of the obtained liquid was measured by squeezing the samples using a flat-bottomed surface electrode, type "Single Pore Fiat", Hamilton. Test Liquid 1 (with reference to Method 2): Synthetic urine containing the following substances: KCl, NaCl, MgSO4, KH2P04, Na2HP04, NH2CONH2. The pH in this composition is 6.0 ± 0.5. The test liquid used is 16 ml synthetic urine (as defined above) for a single absorbent body. The absorbent core preferably comprises at least one layer containing a mixture of fibers and acid superabsorbent material, organic zinc salt and optionally nonacid superabsorbent material.

Non-acidic superabsorbent material (also referred to herein as the standard superabsorbent material) means superabsorbent materials of the type described above with a pH of, for example, 5.8 or greater. Non-acidic SAPs comprising acid group polymerizable units preferably have a degree of neutralization of at least 70%.

The fibers present in the absorbent core are also preferably capable of absorbing body liquids, as in the case of hydrophilic fibers. More preferably, the fibers are cellulosic fibers such as fluff wood pulp, cotton, cotton liners, rayon, cellulose acetate and the like, with the use of fluff cellulosic pulp being preferred. mechanical or chemical type, with chemical pulp being preferred.

In the absorbent core and, if applicable, in each layer thereof, the total amount of superabsorbent material (of the acidic and optionally non-acidic type) is preferably from 10 to 70% w / w, more preferably 20 to 65% w / w, in particular 30 to 60% w / w, for example 30 to 50% w / w, based on the weight of the total blend of fibers and superabsorbent materials (without organic zinc salt). The weight ratio between acidic SAP and non-acidic SAP is not particularly restricted (eg 5/95 to 95/5, 10/90 to 90/10, 20/80 to 80/20), although it appears that larger amounts of SAP acid appear to enhance the effect of the present invention. Accordingly, weight ratios between acidic SAP and non-acidic SAP from 100/0 to 50/50 (e.g. 95/5 to 60/40, 90/10 to 70/30) may preferably be selected depending on the properties to be used. be achieved.

Very low amounts of organic zinc salts already aid acid SAP in very efficient odor control. The lowest preferred weight limit of organic zinc salt (calculated as zinc) appears to be at least 10.5 g per g of dry acid SAP. In this document, the term "dry" used in reference to acid SAP should be understood. as no water having been added thereto, and the only water present therein is the inevitable wastewater from its production process.More preferably, the organic zinc salt is present in amounts of at least 10 -4 g, even more so. preferably at least 5 · 1 (Γ4 g, even more preferably at least 10-3 g. According to the most preferred embodiment, the amount of zinc salt is at least 10 -2 g zinc per g of acid SAP There is no specific upper limit, although for economic reasons a point should be reached where it should no longer be useful to increase zinc content eg to 0.1 or 1 g zinc per g SAP acid if this increase is not accompanied by greater odor suppression.

For example, when the absorbent core contains 40% acid SAP, the concentration of the organic zinc salt may range from 0.03 to 30% w / w.

There are also no specific restrictions on the organic zinc salt used. In accordance with the present invention, zinc salts of organic carboxylic acids having from 2 to 30 carbon atoms, in particular 12 to 24 carbon atoms, are preferably used. The carboxylic acid group may be attached to aliphatic, aliphatic-aromatic, aromatic-aliphatic, alicyclic or aromatic radicals, where the aliphatic chain or alicyclic ring (s) may be unsaturated and are optionally substituted, for example by hydroxy or C1 -C4 alkyl. These salts include zinc acetate, zinc lactate, zinc ricinoleate and zinc abietate. More preferably, the zinc salt is the zinc salt of a hydroxylated unsaturated fatty acid of 8 to 18 carbon atoms. Although there is no specific restriction on the number of unsaturated double bonds or hydroxyl groups, fatty acids having one or two unsaturated double bonds and one or two hydroxyl groups appear to be preferred. The most preferred embodiment is zinc ricinoleate.

According to one embodiment of the present invention, the above described organic zinc salt, such as zinc ricinoleate, is activated by an amino acid, such as TEGO® Sorb A30, commercially available from Degussa. The organic zinc salt used in the present invention may also be capable of removing chemically unpleasant amine-based substances (e.g. nicotine in cigarette smoke), thiocompounds (e.g. allicin in garlic and onions), and of acids (e.g., isovaleric acid in human sweat, and butyric acid). As an example, zinc ricinoleate, which is, for example, sold by Degussa under the trademark TEGO® Sorb, has the additional odor removal effect described and ammonia removal. The present invention is also not subject to any limitations regarding the technique of incorporating organic zinc salt into the absorbent core. However, dipping and spraying are preferred.

For example, it is conceivable to treat the fibers present in the absorbent core, preferably the fluff cellulose pulp, with a solution of the organic zinc salt before or during mixing with acid SAP.

According to a preferred embodiment, a solution of the organic zinc salt is sprayed onto the fibers, more preferably onto the fluff pulp pulp sheets as obtained from the manufacturer. The organic zinc salt solution may be sprayed onto the fluff pulp sheets directly by the manufacturer of said sheets prior to delivery to the absorbent articles manufacturer. This is an especially preferred embodiment since it avoids the extra step of spraying the organic zinc salt solution during production of the absorbent article. Alternatively, the fibers are dipped in the solution. The acid SAP is then added during or after core formation.

Alternatively, a core is formed by conventional fiber techniques, preferably fluff cellulosics, said core being sprayed during core formation with the zinc salt solution. Acid SAP is incorporated either during or after core formation, although it is less preferred to spray the already formed absorbent core. From the presently available information, however, it would appear that the most effective technique for achieving zinc incorporation involves the treatment of an already formed absorbent core comprising a mixture of acid SAP, fibers, preferably fluff cellulose pulp and, optionally, Non-acidic SAP with an organic zinc salt solution, in particular zinc ricinoleate solution.

According to a preferred use technique, the organic zinc salt solution, in particular zinc ricinoleate, is sprayed either on one or both sides of the absorbent core, or on either side of the individual layers constituting the zinc. same. The solvent used for this solution may be water, a preferably organic solvent such as ethanol, or a mixture of water and a water miscible organic solvent such as ethanol. Preferably, the organic zinc solvent is present in the solution at a relatively high concentration, preferably 1 and 30% by weight. The use of such concentrated solutions ensures that the absorptive capacity of superabsorbent material is not reduced further than necessary. Commercially available organic zinc salt solutions, such as TEGO® Sorb Δ30, provided by Degussa (active content 30% by weight, amino acid activated zinc ricinoleate) can also be employed. The bottom layer prevents exudates absorbed by and present in the absorbent layer from staining (soiling) other external articles that may come into contact with the absorbent article, such as sheets and undergarments. In preferred embodiments, the bottom layer is substantially impermeable to liquids (e.g. urine), and comprises a nonwoven laminate and a thin plastic film such as a thermoplastic film having a thickness of about 0.012 mm to about 0.051 mm. mm Suitable backsheet films include those manufactured by Tredegar Industries Inc. of Terre Haute, Ind and sold under the trademarks X15306, X10962, and X10964.

Other suitable lower layer materials may include breathable materials, that is, which allow vapors to be eliminated from the absorbent article and further prevent exudates from passing through the lower layer.

Examples of breathable materials may include materials such as woven blankets, nonwoven blankets, composite materials such as film coated nonwoven blankets, and microporous films.

The above elements of an absorbent article may be assembled, optionally together with other typical absorbent article elements, in a manner known in the art.

The following examples and comparative examples illustrate the present invention. EXAMPLE 1 Circular absorbent test cores, having a weight of about 1.2 g, and a diameter of 5 cm, were obtained from an absorbent core produced in a pilot plant. A standard method of forming a small core mat was used in core production in the pilot plant. The absorbent core consisted of a homogeneous mixture of a fluff pulp and a superabsorbent material. The fluff pulp used was 0.72 g of a Weyerhauser pulp (NB 416), and the superabsorbent material used was 0.48 g of an acid superabsorbent (pH 5.1) called Degussa's Z3106. The absorbent core was compressed to a volume of about 8-10 cm 3 / g.

To the absorbent core 1.3 ml of a 3% w / w zinc ricinoleate solution (supplied by Degussa under the trademark TEGO® Sorb A30, 1/10 dilution) was added, or by dripping the solution onto its surface ( on one side), or by dipping one side of the core into the solution. One week after treatment, the absorbent body absorbed 16 ml of synthetic urine according to Method 3 as described below and was then kept at room temperature. At 4, 6 and 8 hours after absorption of synthetic urine, the amount of ammonia released was measured. Δ mean of five measurements was used as the mean value. The results are shown in Table 1. Method 3: Measurement of ammonia inhibition in absorbent cores Absorbent cores were prepared according to method 1. Test liquid 2 was prepared. Suspension of the bacterium Proteus mirabilis was grown in nutrient broth at 30 ° C overnight. Graft cultures were diluted and bacterial count determined. The final culture contained approximately 105 organisms per ml of liquid tested. The absorbent core was placed in a plastic bottle and test liquid 2 was added to the absorbent core, then the container was incubated at 35 ° C for 4, 6 and 8 hours, respectively, and then samples were taken from the containers using a hand pump and a tube known as the Dragon-tube. Ammonia content was obtained as a color change on a graded scale in ppm or% by volume.

Test Liquid 2: Sterile synthetic urine, to which a medium for growth of microorganisms was added. Synthetic urine contains mono- and divalent cations and anions and urea, and was prepared as described in Geigy, "Scientific Tables", Vol. 2, 8th ed. 1981, page 53. The growth medium for the microorganisms is based on the information from "Hook-and FSA-media for entero-bacteria. The pH in this mixture is 6.6. EXAMPLE 2 An absorbent core was prepared as in Example 1. except that the aqueous solution added thereto, either by dripping the solution onto its surface (on one side) or by dipping one side of the core into the solution, contained 6% by weight of zinc ricinoleate. An absorbent core was prepared as in Example 1, with the one exception that the aqueous solution added thereto, either by dripping the solution onto its surface (on one side), or by dipping one side of the core into the solution, contained 0, 5% by weight of zinc ricinoleate EXAMPLE 4 An absorbent core was prepared as in Example 1, with the sole exception that the aqueous solution added thereto, or by dripping the solution onto its surface (on one side), or plunging one side of the naked core contained in the solution contained 0.3 wt% zinc ricinoleate.

REFERENCE EXAMPLE

An absorbent body was prepared as in Example 1, with the one exception that the acid superabsorbent was replaced by a conventional nonacid superabsorbent (Dow XZS 91030.03, supplied by Dow Chemical). In addition, no treatment with zinc ricinoleate was performed. COMPARATIVE EXAMPLE 1 An absorbent core was prepared as in Example 1, with the one exception that the acid superabsorbent was replaced by a nonacid type (Dow XZS 91030.03, supplied by Dow Chemical). COMPARATIVE EXAMPLE 2 An absorbent body was prepared as in Example 1, with the only difference that no treatment with a zinc ricinoleate solution was performed.

The ammonia formation results of the reference example, Comparative Examples 1 and 2, and Examples 1 to 4 are shown in Table 1 below. EXAMPLE 5 An absorbent core was prepared as in Example 1, with the only exception that the commercially available acid superabsorbent M7125 (BASF, pH = 4.9 ± 0.2) was used instead of Degussa's Z3106. COMPARATIVE EXAMPLE 3 An absorbent core was prepared as in Example 5, with the sole exception that no zinc ricinoleate was added thereto.

The ammonia formation results of Comparative Example 3 and Example 5 are shown in Table 2 below.

The above experiments show that the combined use of an acid superabsorbent and an organic zinc salt, such as zinc ricinoleate, eliminates ammonia formation to a very surprising degree. Considering the fact that a human being can detect ammonia smell at a concentration of 30 ppm, the present invention ensures that during use of an absorbent article no ammonia odor will be felt by the user.

Claims (9)

1. An absorbent article, such as a diaper, a daily hygienic protector, a female tampon or urinary incontinence diaper, comprising a liquid-permeable topsheet, a liquid-impermeable bottomsheet and an absorbent core situated between the two aforementioned layers, where the It further comprises a superabsorbent material, characterized in that said superabsorbent material is an acidic superabsorbent material having a pH of 5.5 or less, and in that the absorbent core further comprises zinc ricinoleate. An absorbent article according to claim 1, wherein the absorbent core comprises a fiber blend, in particular Fluff cellulose pulp, acid superabsorbent material and optionally non-acid superabsorbent material. Absorbent core according to claim 1 or 2, wherein the total amount of acid and non-acid superabsorbent material is 10 to 70% by weight based on the weight of the core (excluding organic zinc salt) , An absorbent core according to claim 2 or 3, wherein the acid superabsorbent is present in an amount of at least 501 by weight based on the total amount of superabsorbent materials. An absorbent article according to any one of claims 1 to 4, wherein the amount of organic zinc salt is at least ΙΟ5.5 g of Zn per g of dry acid superabsorbent material. An absorbent article according to any one of claims 1 to 5, wherein it is obtained by treating the absorbent core with an organic zinc salt solution. 7. Absorbent article according to. any one of claims 1 to 6, wherein the absorbent core has a pH value of 3.0 to 5.7, preferably 3.5 to 5.5, in particular 4.1 to 5.4, after being soaked with urine synthetic. An absorbent article according to any one of claims 1 to 6, wherein the acid superabsorbent material has a pH value of 3.0 to 5.5, preferably 3.5 to 5.3, and more preferably 4; 1 to 5.2. An absorbent article according to any one of claims 1 to 8, wherein the acid superabsorbent material is a crosslinked homo- or copolymer comprising (meth) acrylic acid units.